chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124635881124635882GC12GENIChomozygous936924860
X124636223124636224GA14GENIChomozygous936924861
X124642452124642453AG14GENIChomozygous936924862
X124643201124643202CT12GENIChomozygous936924863
X124644532124644533CT27GENIChomozygous936924864
X124644755124644756CT22GENIChomozygous936924865
X124648028124648029GT19GENIChomozygous936924866
X124648043124648044CT21GENIChomozygous936924867
X124648547124648548AG16GENIChomozygous936924868
X124648836124648837TC11GENIChomozygous936924869
X124651865124651866GC10GENIChomozygous936924870
X124651980124651981CT20GENIChomozygous936924871